培马巴贝特对代谢功能障碍相关脂肪变性肝病患者血清肉碱和血浆肌生长抑制素的影响

Ryohei Tanigawa, Atsushi Nakajima, Yuichiro Eguchi, Hirokazu Takahashi, Rohit Loomba, Hideki Suganami, Masaya Tanahashi, Hidenori Arai
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引用次数: 0

摘要

背景:在代谢功能障碍相关脂肪变性肝病(MASLD)患者的pama - fl研究中,Pemafibrate是一种选择性过氧化物酶体增殖物激活受体α (PPARα)调节剂(SPPARMα),对肝脏相关标志物(例如,通过磁共振弹性成像和丙氨酸转氨酶测定的肝脏硬度)具有积极作用。据报道,MASLD患者的肌肉质量损失率很高;因此,预防和治疗肌少症对MASLD患者至关重要。PPARα可能参与肉碱和肌肉生长抑制素的表达,这是已知的肌肉相关标志物。我们对pama - fl研究进行了事后分析,以调查培马布特对肉碱和肌肉生长抑制素水平的影响。poma - fl研究是一项双盲、安慰剂对照、随机、多中心、2期试验,118例患者随机分为poma - fl组(0.4 mg/d)和安慰剂组(1:1)(口服,每日2次,持续72周)。这个事后分析检查了与安慰剂组相比,培马哌特组中总肉毒碱、游离肉毒碱、酰基肉毒碱和肌肉生长抑制素的百分比变化。我们检查了肉毒碱和肌肉生长抑制素水平百分比变化之间的相关性。结果在第48周,与安慰剂相比,pmafitate显著增加了血清总肉毒碱和游离肉毒碱水平(治疗差异24.2%;P < 0.001, 27.3%;P < 0.001),血清酰基肉碱的趋势相似(治疗差异为10.7%)。在第72周,培马哌特显著降低血浆肌生长抑制素水平(治疗差异为- 11.0%;P < 0.01)。分析各组游离肉碱和肌肉生长抑制素水平的显著变化,发现几乎所有亚组的变化都相似。血清总肉毒碱、游离肉毒碱和酰基肉毒碱与血浆肌生长抑制素在12周的变化百分比无明显相关性(r = 0.337, r = 0.358, r = 0.077)。结论培马菲特可提高MASLD患者血清肉碱水平,降低血浆肌生成抑制素水平,可能在肌少症的发生发展中有潜在的应用价值,但对肌肉质量的影响尚无结果。需要进一步的研究来确定这些生理变化是否能在预防或治疗MASLD患者肌肉减少症方面带来临床益处。试验注册:ClinicalTrials.gov标识符:NCT03350165。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of Pemafibrate on Serum Carnitine and Plasma Myostatin in Patients With Metabolic Dysfunction Associated Steatotic Liver Disease

Effects of Pemafibrate on Serum Carnitine and Plasma Myostatin in Patients With Metabolic Dysfunction Associated Steatotic Liver Disease

Background

Pemafibrate, a selective peroxisome proliferator-activated receptor alpha (PPARα) modulator (SPPARMα), has positive effects on liver-related markers (e.g., liver stiffness determined by magnetic resonance elastography and alanine aminotransferase) in the PEMA-FL study in patients with metabolic dysfunction-associated steatotic liver disease (MASLD). Patients with MASLD reportedly have a high rate of muscle mass loss; hence, the prevention and treatment of sarcopenia is important for patients with MASLD. PPARα may be involved in the expression of carnitine and myostatin, which are known muscle-related markers. We conducted a post-hoc analysis of the PEMA-FL study to investigate the effects of pemafibrate on carnitine and myostatin levels.

Methods

The PEMA-FL study, a double-blind, placebo-controlled, randomized, multicenter, Phase 2 trial, randomized 118 patients to either Pemafibrate 0.4 mg/day or placebo (1:1) group (orally, twice daily for 72 weeks). This post-hoc analysis examined the percentage change in total carnitine, free carnitine, acylcarnitine, and myostatin in the pemafibrate group compared to those in the placebo group. We examined the correlation between percentage changes in carnitine and myostatin levels.

Results

Pmafibrate significantly increased serum total carnitine and free carnitine levels from baseline compared to placebo at Week 48 (treatment difference 24.2%; p < 0.001, 27.3%; p < 0.001, respectively) with similar trends for serum acylcarnitine (treatment difference 10.7%). Pemafibrate significantly reduced plasma myostatin levels at Week 72 (treatment difference −11.0%; p < 0.01) from baseline. Analysis of the significant changes in free carnitine and myostatin levels by subgroups showed similar changes in almost all subgroups. The percent changes in the serum total carnitine, free carnitine and acylcarnitine, and plasma myostatin levels at 12 weeks demonstrated no obvious correlations (r = 0.337, r = 0.358, r = 0.077, respectively).

Conclusions

Pemafibrate increased the serum carnitine and decreased plasma myostatin levels in patients with MASLD, which may have potential application in the development and progression of sarcopenia, but there are no results on the effect on muscle mass. Further research is warranted to determine whether these changes in physiology can lead to clinical benefits in the prevention or treatment of sarcopenia in patients with MASLD.

Trial Registration: ClinicalTrials.gov identifier: NCT03350165.

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